Miller WL - Search Results

1

Clinical review 54: Genetics, diagnosis, and management of 21-hydroxylase deficiency.

Miller WL. Miller WL. J Clin Endocrinol Metab. 1994 Feb;78(2):241-6. doi: 10.1210/jcem.78.2.8106606. J Clin Endocrinol Metab. 1994. PMID: 8106606 Review. No abstract available.

2

Normal genes for the cholesterol side chain cleavage enzyme, P450scc, in congenital lipoid adrenal hyperplasia.

Lin D, Gitelman SE, Saenger P, Miller WL. Lin D, et al. Among authors: miller wl. J Clin Invest. 1991 Dec;88(6):1955-62. doi: 10.1172/JCI115520. J Clin Invest. 1991. PMID: 1661294 Free PMC article.

3

Missense mutation serine106----proline causes 17 alpha-hydroxylase deficiency.

Lin D, Harikrishna JA, Moore CC, Jones KL, Miller WL. Lin D, et al. Among authors: miller wl. J Biol Chem. 1991 Aug 25;266(24):15992-8. J Biol Chem. 1991. PMID: 1714904 Free article.

4

Congenital adrenal hyperplasias.

Miller WL. Miller WL. Endocrinol Metab Clin North Am. 1991 Dec;20(4):721-49. Endocrinol Metab Clin North Am. 1991. PMID: 1778175 Review.

5

Human proopiomelanocortin-(79-96), a proposed androgen stimulatory hormone, does not affect steroidogenesis in cultured human fetal adrenal cells.

Mellon SH, Shively JE, Miller WL. Mellon SH, et al. Among authors: miller wl. J Clin Endocrinol Metab. 1991 Jan;72(1):19-22. doi: 10.1210/jcem-72-1-19. J Clin Endocrinol Metab. 1991. PMID: 1846003

6

Tissue-specific, cyclic adenosine 3',5'-monophosphate-induced, and phorbol ester-repressed transcription from the human P450c17 promoter in mouse cells.

Brentano ST, Picado-Leonard J, Mellon SH, Moore CC, Miller WL. Brentano ST, et al. Among authors: miller wl. Mol Endocrinol. 1990 Dec;4(12):1972-9. doi: 10.1210/mend-4-12-1972. Mol Endocrinol. 1990. PMID: 1964490

7

Immunoassays for human müllerian inhibitory factor (MIF): new insights into the physiology of MIF.

Miller WL. Miller WL. J Clin Endocrinol Metab. 1990 Jan;70(1):8-10. doi: 10.1210/jcem-70-1-8. J Clin Endocrinol Metab. 1990. PMID: 2403573 Review. No abstract available.

8

Molecular characterization of a Leydig cell tumor presenting as congenital adrenal hyperplasia.

Solish SB, Goldsmith MA, Voutilainen R, Miller WL. Solish SB, et al. Among authors: miller wl. J Clin Endocrinol Metab. 1989 Dec;69(6):1148-52. doi: 10.1210/jcem-69-6-1148. J Clin Endocrinol Metab. 1989. PMID: 2555382

9

The molecular genetics of 21-hydroxylase deficiency.

Miller WL, Morel Y. Miller WL, et al. Annu Rev Genet. 1989;23:371-93. doi: 10.1146/annurev.ge.23.120189.002103. Annu Rev Genet. 1989. PMID: 2694937 Review. No abstract available.

10

Gene conversions and rearrangements cause discordance between inheritance of forms of 21-hydroxylase deficiency and HLA types.

Morel Y, David M, Forest MG, Betuel H, Hauptman G, Andre J, Bertrand J, Miller WL. Morel Y, et al. Among authors: miller wl. J Clin Endocrinol Metab. 1989 Mar;68(3):592-9. doi: 10.1210/jcem-68-3-592. J Clin Endocrinol Metab. 1989. PMID: 2783935

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